ArticleISRN endocrinology2013
Growth and specialized growth charts of children with congenital hypothyroidism detected by neonatal screening in isfahan, iran.
Article in ISRN endocrinology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed.
- Effect of timely diagnosis and treatment on growth and body proportionality of children with congenital hypothyroidism.Frontiers in endocrinology · 2025Article
- Establishing Localized Growth Velocity Standards for Children: A Study from Isfahan.Advanced biomedical research · 2025Article
- Growth Pattern of Preterm Neonates with Fetal Growth Restriction: A Prospective Cohort Study.Indian journal of pediatrics · 2024Article
- The longitudinal growth trajectory of children with congenital hypothyroidism during the first 3 years of life.European journal of pediatrics · 2024Article
- Postnatal Serum Total Thyroxine Level Associated with Short- and Long-Term Anthropometric Outcomes in Very Preterm Infants.Nutrients · 2022Article
- Evaluation of the developmental outcome in children with congenital hypothyroidism.Caspian journal of internal medicine · 2021Article
- Final height of Korean patients with early treated congenital hypothyroidism.Korean journal of pediatrics · 2018Article
- A 7-year study on the prevalence of congenital hypothyroidism in northern Iran.Electronic physician · 2018Article
- Article
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Authors and funding
9 authors.
Funding
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Abstract
Objectives. The aim of the current study was to investigate the growth status of CH, generate specialized growth charts of CH infants, and compare them with their counterparts of regional normal infants. Methods. In this prospective cohort study, 760 (345 girls and 415 boys) neonates born in 2002-2009 diagnosed by neonatal CH screening program in Isfahan were followed up from the time of diagnosis. 552 healthy children were recruited as a control group. The empirical 3rd, 15th, 50th, 85th, and 97th percentiles for height, weight, and head circumference of both sexes were determined and compared with their counterpart values of the control group. The relative frequency of patients with impaired growth for each studied variable was determined. Also, specialized growth charts of CH patients were generated. Results. The percentiles of weight, height, and head circumference of studied patients are significantly different from regional healthy children (P < 0.001). The relative frequency of impaired head circumference was decreased to less than 3% at the 3rd year of age and for height it reached gradually 3% and 9% at the 5th year of age for boys and girls, respectively (P < 0.05); however for weight still it was statistically more than 3% in both sexes. Conclusion. CH patients had impaired growth development which was improved during follow up, but the catch-up time was earlier for head circumference and later for weight.
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Registered trials
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